Proteomics

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DUX4 interactors by LC-MSMS


ABSTRACT: The aim of this study is to define the molecular mechanisms underlying DUX4-associated toxicity in the context of facioscapulohumeral muscular dystrophy (FSHD). DUX4 is a transcription factor, which induces cell death by activating the transcription of its targets. No molecule able to directly control DUX4 activity is currently known. By using a tandem affinity purification protocol combined to mass spectrometry analysis, we identified Matrin 3 (MATR3), as the first cellular factor able to directly block DUX4 toxic activity. We found that MATR3 binds to the DNA binding domain of DUX4 blocking the activation of its genomic targets.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Annapaola Andolfo  

LAB HEAD: Davide Gabellini

PROVIDER: PXD011073 | Pride | 2023-08-21

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
F004285.mzid.gz Mzid
F004285.pride.mztab.gz Mztab
F004286.mzid.gz Mzid
F004286.pride.mztab.gz Mztab
F004287.mzid.gz Mzid
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